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Observation of laser-induced electronic structure in oriented polyatomic molecules.


ABSTRACT: All attosecond time-resolved measurements have so far relied on the use of intense near-infrared laser pulses. In particular, attosecond streaking, laser-induced electron diffraction and high-harmonic generation all make use of non-perturbative light-matter interactions. Remarkably, the effect of the strong laser field on the studied sample has often been neglected in previous studies. Here we use high-harmonic spectroscopy to measure laser-induced modifications of the electronic structure of molecules. We study high-harmonic spectra of spatially oriented CH3F and CH3Br as generic examples of polar polyatomic molecules. We accurately measure intensity ratios of even and odd-harmonic orders, and of the emission from aligned and unaligned molecules. We show that these robust observables reveal a substantial modification of the molecular electronic structure by the external laser field. Our insights offer new challenges and opportunities for a range of emerging strong-field attosecond spectroscopies.

SUBMITTER: Kraus PM 

PROVIDER: S-EPMC4432593 | biostudies-literature | 2015 May

REPOSITORIES: biostudies-literature

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Observation of laser-induced electronic structure in oriented polyatomic molecules.

Kraus P M PM   Tolstikhin O I OI   Baykusheva D D   Rupenyan A A   Schneider J J   Bisgaard C Z CZ   Morishita T T   Jensen F F   Madsen L B LB   Wörner H J HJ  

Nature communications 20150505


All attosecond time-resolved measurements have so far relied on the use of intense near-infrared laser pulses. In particular, attosecond streaking, laser-induced electron diffraction and high-harmonic generation all make use of non-perturbative light-matter interactions. Remarkably, the effect of the strong laser field on the studied sample has often been neglected in previous studies. Here we use high-harmonic spectroscopy to measure laser-induced modifications of the electronic structure of mo  ...[more]

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